PH31206A - Process for the preparation of a cephalosporin antibiotic. - Google Patents

Process for the preparation of a cephalosporin antibiotic.

Info

Publication number
PH31206A
PH31206A PH44905A PH44905A PH31206A PH 31206 A PH31206 A PH 31206A PH 44905 A PH44905 A PH 44905A PH 44905 A PH44905 A PH 44905A PH 31206 A PH31206 A PH 31206A
Authority
PH
Philippines
Prior art keywords
preparation
isomer
methyl
cephalosporin antibiotic
antibiotic
Prior art date
Application number
PH44905A
Inventor
Gary M F Lim
John M Roubie
Elizabeth A Garofalo
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of PH31206A publication Critical patent/PH31206A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/38Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C07D501/46Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Revetment (AREA)
  • Artificial Fish Reefs (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Ultra Sonic Daignosis Equipment (AREA)

Abstract

The present invention provides an anhydrous acylation process for the preparation of antibiotic, cefepime dihydrochloride hydrate which is substantially free of the anti-isomer and the DELTA <2> isomer comprising the N-acylation of a silylated derivative of 7-amino-3-[(1-methyl-1-pyrrolidinio)-methyl]ceph-3-em-4-carboxylate with the syn-isomer of 2-(2-aminothiazol-4-yl)-2-methoxyimino acetyl chloride hydrochloride.
PH44905A 1991-09-10 1992-09-09 Process for the preparation of a cephalosporin antibiotic. PH31206A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US75710491A 1991-09-10 1991-09-10

Publications (1)

Publication Number Publication Date
PH31206A true PH31206A (en) 1998-05-05

Family

ID=25046366

Family Applications (1)

Application Number Title Priority Date Filing Date
PH44905A PH31206A (en) 1991-09-10 1992-09-09 Process for the preparation of a cephalosporin antibiotic.

Country Status (29)

Country Link
EP (1) EP0531981B1 (en)
JP (1) JP3434840B2 (en)
KR (1) KR0178280B1 (en)
CN (2) CN1036587C (en)
AT (1) ATE209209T1 (en)
AU (1) AU655838B2 (en)
BG (1) BG61189B1 (en)
CA (1) CA2077836A1 (en)
CZ (2) CZ71996A3 (en)
DE (1) DE69232216T2 (en)
DK (1) DK0531981T3 (en)
EG (1) EG20184A (en)
ES (1) ES2165351T3 (en)
FI (2) FI109127B (en)
HU (1) HU212782B (en)
IL (1) IL103109A (en)
MX (1) MX9205147A (en)
NO (1) NO301930B1 (en)
NZ (1) NZ244295A (en)
OA (1) OA09764A (en)
PH (1) PH31206A (en)
PL (1) PL174820B1 (en)
PT (1) PT531981E (en)
RO (1) RO109651B1 (en)
RU (1) RU2042681C1 (en)
SK (2) SK280934B6 (en)
UY (1) UY23475A1 (en)
YU (1) YU81692A (en)
ZA (1) ZA926866B (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY108872A (en) * 1991-09-10 1996-11-30 Bristol Myers Squibb Co Preparation of a cephalosporin antibiotic using the syn-isomer of a thiazolyl intermediate.
CA2101571A1 (en) * 1992-09-08 1994-03-09 Elizabeth A. Garofalo Crystalline dihydrate of a cephalosporin dihydrate salt and injectable compositions thereof
KR19980019860A (en) * 1996-09-04 1998-06-25 김윤배 New Manufacturing Method of Cephalosporin Intermediates
ATE473986T1 (en) * 2003-04-16 2010-07-15 Sandoz Ag METHOD FOR PRODUCING CEFEPIM
US7847093B2 (en) 2003-04-16 2010-12-07 Sandoz Ag Processes for the preparations of cefepime
GB0416379D0 (en) * 2004-07-22 2004-08-25 Sandoz Ag Organic compounds
ITMI20051684A1 (en) * 2005-09-13 2007-03-14 Harvest Lodge Ltd PROCEDURE FOR THE PRODUCTION OF AMINO ACID DICHLORIDRATE
RU2469040C1 (en) * 2011-12-07 2012-12-10 Общество с ограниченной ответственностью "КОМПАНИЯ "ДЕКО" Method of producing 7-[2-(2-aminothiazol-4-yl)-2(z)-methoxyimino acetamido]-3-[(1-methyl-1-pyrrolidino)methyl]-cef-3-em-4-carboxylate dihydrochloride monohydrate (cefepime dihydrochloride monohydrate)

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1213882A (en) * 1982-03-04 1986-11-12 Jun Okumura Cephalosporins
DE3419015A1 (en) * 1984-05-22 1985-11-28 Bayer Ag, 5090 Leverkusen METHOD FOR PRODUCING CEPHALOSPORINES
GB2165245B (en) * 1984-10-01 1988-05-25 Glaxo Group Ltd Chemical compounds
US4910301A (en) * 1985-08-05 1990-03-20 Bristol-Myers Company Cefepime cephalosporin salts
US4714760A (en) * 1985-08-20 1987-12-22 Bristol-Myers Company Cephalosporin intermediates
MY108872A (en) * 1991-09-10 1996-11-30 Bristol Myers Squibb Co Preparation of a cephalosporin antibiotic using the syn-isomer of a thiazolyl intermediate.

Also Published As

Publication number Publication date
EP0531981B1 (en) 2001-11-21
YU81692A (en) 1995-03-27
JP3434840B2 (en) 2003-08-11
UY23475A1 (en) 1992-10-08
ES2165351T3 (en) 2002-03-16
HU9202884D0 (en) 1992-11-30
FI119811B (en) 2009-03-31
RO109651B1 (en) 1995-04-28
BG61189B1 (en) 1997-02-28
JPH05194532A (en) 1993-08-03
PL295873A1 (en) 1993-05-04
EP0531981A1 (en) 1993-03-17
ATE209209T1 (en) 2001-12-15
NO301930B1 (en) 1997-12-29
CZ282160B6 (en) 1997-05-14
NZ244295A (en) 1995-08-28
DK0531981T3 (en) 2002-05-21
EG20184A (en) 1997-09-30
IL103109A0 (en) 1993-02-21
OA09764A (en) 1993-11-30
DE69232216D1 (en) 2002-01-03
NO923495L (en) 1993-03-11
CA2077836A1 (en) 1993-03-11
CZ278092A3 (en) 1993-03-17
PT531981E (en) 2002-05-31
CN1158333A (en) 1997-09-03
ZA926866B (en) 1993-03-09
FI924031A (en) 1993-03-11
SK33698A3 (en) 2000-09-12
SK280933B6 (en) 2000-09-12
MX9205147A (en) 1993-03-01
CN1036587C (en) 1997-12-03
RU2042681C1 (en) 1995-08-27
BG96859A (en) 1993-12-24
NO923495D0 (en) 1992-09-09
CN1070398A (en) 1993-03-31
CZ282315B6 (en) 1997-06-11
AU2284492A (en) 1993-03-11
FI20011921A (en) 2001-10-01
FI924031A0 (en) 1992-09-09
HU212782B (en) 1996-11-28
SK280934B6 (en) 2000-09-12
CN1059438C (en) 2000-12-13
KR930006032A (en) 1993-04-20
PL174820B1 (en) 1998-09-30
CZ71996A3 (en) 1997-06-11
SK278092A3 (en) 2000-09-12
IL103109A (en) 1997-07-13
KR0178280B1 (en) 1999-03-20
DE69232216T2 (en) 2002-06-27
AU655838B2 (en) 1995-01-12
FI109127B (en) 2002-05-31
HUT62901A (en) 1993-06-28

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EG20184A (en) Process for the preparation of a cephalosporin antibiotic
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